A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520151



Internal ID15447444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54487871..54503066hg38UCSC Ensembl
Innerchr10:56247631..56262826hg19UCSC Ensembl
Innerchr10:55917637..55932832hg18UCSC Ensembl
Innerchr10:55917637..55932832hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3815196
hg1915196
hg1815196
hg1715196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674402, nssv661249
Samples
Known GenesPCDH15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520151
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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